NDC 21695-630
Terbinafine Hydrochloride 250 mg tablet
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Aurobindo Pharma Limited's NDC 65862-079.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet
- Strength
- 250 mg
- Approval
- ANDA ANDA077533
- On the market since
- Jul 2, 2007
- Package NDCs
21695-630-3021695-630-4221695-630-4521695-630-6021695-630-90- Official label
- DailyMed (National Library of Medicine), updated Feb 9, 2011
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